Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs688325 0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs806371 0.882 0.040 6 88146644 intron variant T/G snv 0.18 4
rs853679 0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs9394309 0.851 0.040 6 35654004 intron variant G/A snv 0.74 4
rs11082011 0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs11155372 0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs112106319 0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs11924809 0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs11989919 0.882 0.040 8 32645107 intron variant T/C snv 0.10 3
rs11990063 0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs12278912 0.882 0.040 11 124742263 intron variant G/A snv 0.33 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs139459337 0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs142484554 0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502 0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs1432441 0.882 0.040 15 66426943 intron variant G/A snv 0.27 3
rs143405544 0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs1541187 0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs1549854 0.882 0.040 15 66404397 intron variant A/C;G snv 0.44 3
rs17236239 0.882 0.040 7 147885213 intron variant A/G snv 0.26 3
rs183042538 0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs188843168 0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs189864513 0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3